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All Journal Jurnal Gizi dan Pangan ACTA VETERINARIA INDONESIANA Hemera Zoa Media Veteriner Forum Pasca Sarjana Jurnal Sain Veteriner Buletin Peternakan Majalah Ilmiah Peternakan Jurnal Veteriner Microbiology Indonesia BIOTROPIA - The Southeast Asian Journal of Tropical Biology Media Gizi Mikro Indonesia Jurnal Ilmu-Ilmu Peternakan (Indonesian Journal of Animal Science) Jurnal Ilmu Ternak Veteriner Jurnal Riset Veteriner Indonesia (Journal of The Indonesian Veterinary Research) GIZI INDONESIA Animal Production : Indonesian Journal of Animal Production Jurnal Ilmu Nutrisi dan Teknologi Pakan Jurnal Teknologi & Industri Hasil Pertanian Indonesian Aquaculture Journal Jurnal Medik Veteriner ARSHI Veterinary Letters Amerta Nutrition JURNAL KAJIAN VETERINER Jurnal Kedokteran Hewan The International Journal of Tropical Veterinary and Biomedical Research
I wayan Teguh Wibawan
Departemen Ilmu Penyakit Hewan Dan Kesehatan Masyarakat Veteriner Fakultas Kedokteran Hewan, Institut Pertanian Bogor Jl Agathis, Kampus IPB Dramaga, Bogor, Jawa Barat, Indonesia 16680
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Uji Patogenisitas Zoospora Kapang Lagenidium giganteum terhadap Larva Instar-2 Nyamuk Aedes aegypti Skala Laboratorium (PATHOGENICITY TEST OF ZOOSPORA LAGENIDIUM GIGANTEUM FUNGI AGAINST AEDES AEGYPTI LARVAE 2nd UNDER LABORATORY CONDITION) Agustin Indrawati; Mirnawati Sudarwanto; Mangaraja Pidoli Tampubolon; Retno Damayanti Soejoedono; I Wayan Teguh Wibawan
Jurnal Veteriner Vol 12 No 1 (2011)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Dengue Haemorrhagic fever (DHF) is one of fearsome diseases in society. Incidence of the disease isincreasing. Dengue fever is caused by dengue virus and transmitted by Aedes aegypti mosquito vector.Various chemical controls have been conducted to prevent the spread of the disease, but active contents ofthe chemical controlling substances are suspected causing many negative effect, in environment, such asvector resistance, death of non target living creatures, and environmental contamination.This researchobjective was to find an alternative solution in order to control the dengue vector by using entomopathogenicfungi as biological control agent. This research was conducted by isolation and identification of fungiinfecting mosquito larvae. Macroscopic observation revealed that one of the nine isolation products wasLagenidium giganteum. The effectiveness test in laboratory showed the zoospore LD50 to Ae.aegypti larvaeof instar 2nd was 2,35 x 106 zoospore/ml, while the LD95 value was 1,35 x 107 zoospore/ml. The oosporeeffectiveness test showed LD50 was 6,7 x 102 oospore/ml and LD95 was 1,94 x 103 oospore/ml. Using LPCBdye and blue tolouidin 2,5%, the infection mechanism of L.giganteum fungi in Ae.aegypti mosquito larvawas detected. The research is concluded that the entomophatogen fungi L. giganteum was very prospectiveto be used as a biological control agent against vector of DHF.
Relation Between Encapsulation and Adherence Properties of Bacteria Streptococci of Serological Group B to DEAE-Sephacel (HUBUNGAN ANTARA KEBERADAAN KAPSUL DENGAN SIFAT ADHESIFITAS BAKTERI STREPTOKOKUS GRUP B PADA DEAE-SEPHACEL) Fachriyan Pasaribu; I Wayan Teguh Wibawan; Christoph Lammler
Jurnal Veteriner Vol 4 No 1 (2003)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Aktivitas IgY dan IgG Antitetanus setelah Perlakuan pada Berbagai pH, Suhu dan Enzim Proteolitik I Gusti Ayu Agung Suartini; I Wayan Teguh Wibawan; Maggy T. Suhartono; Supar -; I Nyoman Suarta
Jurnal Veteriner Vol 8 No 4 (2007)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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A study was carried out to find out an alternative method of producing antitetanus antibody (IgY) in chicken and to evaluate its activity at different levels of pH, temperatures and proteolytic enzymes. Antitetanus IgY was produced by immunization of chickens with tetanus toxoid, three times weekly at gradual doses of 100, 200, and 300 Lf, respectively. Serum samples were collected 4 weeks following the last immunization. IgY was purified by ammonium sulfat precipitation and gel filtration chromatography (Sephadex G. 120).The purified IgY was then treated at different levels of temperatures and pH as well as proteolytic enzymes. Commercial antitetanus IgG was used as control. The activities of treated IgY and IgG were tested by enzyme linked immunosorbent assay (ELISA). IgY and IgG activities were significantly reduced at 80ºC and completely destroyed at 90ºC. Treatment with pepsin significantly reduced IgY and IgG whereas trypsin slightly reduced IgY activities and has no effect on IgG activities. IgY and IgG activities were reduced significantly at pH < 3 and and only sightly reduced at pH>10. It is evident that heating at >90oC, pH at <3 and treatment with pepsin significantly reduced IgY activities and it appears that IgG was more resistent to the efect of temperatures, pH and proteolytic enzymes
Resistensi Antibiotik pada Salmonella Isolat Sapi Bakalan Asal Australia yang Diimpor Melalui Pelabuhan Tanjung Priok Jakarta (ANTIBIOTIC RESISTANCE OF SALMONELLA ISOLATES FROM AUSTRALIAN IMPORTED FEEDER CATTLES THROUGH TANJUNG PRIOK PORT JAKARTA) Anindya Kurniawati; Denny Widaya Lukman; I Wayan Teguh Wibawan
Jurnal Veteriner Vol 17 No 3 (2016)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Importation of feeder cattle from farms constantly using antibiotics in feed could result in the occurrenceof antibiotic resistant bacteria. A study was therefore conducted to investigate the possible use antibioticsand the antibiotic resistance of commensal Salmonella sppagainst several antibiotics. Salmonella spp.bacteria (n=50)were isolated from 100 samples of feeder cattlesfaeces. Total of 50 Salmonella spp. isolateswere subjected for Salmonella spp. examination and the isolated Salmonella spp. was tested for theantibiotic resistance using 10 antibiotics (ampicillin, cephalotin, erythromycin, tetracycline, streptomycin,chloramphenicol, trimethoprim, trimethoprim-sulfamethoxazole, nalidixic acid, and enrofloxacin) usingdisk diffusion method on Muller-Hinton agar following Clinical and Laboratory Standards Institute (CLSI)guidelines for interpretation. The isolated Salmonella showed resistance towards erythromycin 98%,ampicillin 34%, streptomycin 22%, nalidixic acid 8%, cephalotin 6%, tetracycline 4%, and chloramphenicol2%. There was no resistance against enrofloxacin, trimethoprim, and trimethoprim-sulfamethoxazole. Salmonella spp. bacteria derived from imported feeder cattle which have been resistant to antibiotics arepotential for spreading the antibiotic resistant bacteria to other susceptible animals. Such bacteria canalsotransfer the antibiotic resistant gene to other bacteria in Indonesia which ould be a potential threatfor public and animal healths.
Vaksin Polivalen Untuk Mencegah Penyakit Flu Burung (POLIVALEN VACCINE TO PREVENT BIRD FLU DISEASES) I Nyoman Suartha; I Wayan Wirata; I Gusti Ngurah Narendra Putra; Ni Made Ritha Krisna Dewi; I Made Suma Anthara; I Wayan Teguh Wibawan; I Gusti Ngurah Kade Mahardika
Jurnal Veteriner Vol 13 No 2 (2012)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Abstract

This study was carried out to determine the use of bird flu polyvalent vaccines containing two or threeor more virus isolates representating of circulating viruses in the region. Three seed isolates of avianinfluenza H5N1 virus were used in this experiment. The isolates were Chicken/Denpasar/Unud-01/2004,Chicken/Klungkung/Unud-12/2006, and Chicken/Jembrana/Unud-17/2006. The seeds were inactivatedusing 0.01% formaldehide than mixed (AI3G) alumunium hidroxide adjuvant and then injectedintramuscularly to Isa Brown layer chicken at 3 weeks of age and repeated at the age of 5 weeks. The doseof each seed virus was 27 HA units. Sera were collected at one and two weeks after the second vaccination.The result showed that the arithmetic meant titer (AMT) of sera that tested with homologous isolate washigher than the test using a heterologous isolates, in the standard haemaglutination inhibition (HI) assay.The mixed AI3G vaccine produced a uniform AMT against the constituent isolates, while vaccines withindividual isolate yielded a lower and more variation in AMT. Further experiments using a commercialhomologous H5N1 and heterologous H5N2 commercial vaccines has resulted AMT that 1-4 log lower thanAI3G vaccine. It is concluded that polyvalent vaccine with field seed isolates is recommended to be appliedin the poultry farm in Indonesia.
Perbandingan Sekuens Konsensus Gen Hemaglutinin Virus Avian Influenza Subtipe H5N1 Asal Unggas di Indonesia dengan Subtipe H5N2 dan H5N9 I Gusti Ngurah Kade Mahardika; I Nyoman Suartha; Ida Bagus Kade Suardana; I Gusti Ayu Yuniati Kencana; I Wayan Teguh Wibawan
Jurnal Veteriner Vol 10 No 1 (2009)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Abstract

Consensus sequence of hemagglutinin (HA) gene of avian influenza viruses of H5N1 subtype isolatedfrom fowl in Indonesia – hereafter named as H5N1_Indonesia – is compared with that of H5N2 and H5N9viruses. Sequence information were downloaded from the public database GeneBank. The genetic distancesand nucleotide as well as its deduced amino-acid sequence alignment were analysed. At nucleotide level,genetic distances of HA between H5N1_Indonesia to H5N2 and H5N9 are 16.2% and 9.6%, respectively.At amino-acid level, the distances are 9.7% and 6.8%. The genetic distances of HA1 fragments are 19.0%(H5N1_Indonesia – H5N2) and 10.9% (H5N1_Indonesia – H5N9). At amino-acid, level the genetic distancesof HA1 are 13.1% (H5N1_Indonesia-H5N2) and 8.8% (H5N1_Indonesia – H5N9). All three subtypes havedifferent glycosilation motive and variation of amino-acid sequence of four antigenic sites. The consequenceof those facts is discussed.
SEKUENSING GEN MCR-1 DARI ESCHERICHIA COLI DAN SALMONELLA ENTERITIDIS RESISTAN KOLISTIN Maria Fatima Palupi; Ernes Andhesfa; Hera Maheshwari; Huda Salahuddin Darusman; Etih Sudarnika; I Wayan Teguh Wibawan
Jurnal Veteriner Vol 21 No 3 (2020)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Gen mobilized colistin resistance (mcr) merupakan gen resistan kolistin sulfat yang bisa dipindahkan melalui materi genetik bergerak misalnya plasmid. Tujuan dari penelitian ini adalah mengetahui jenis plasmid gen mcr-1 yang berhasil dipindahkan dari satu isolat Escherichia coli resistan kolistin ke Salmonella Enteritidis ATCC 13076 (dua isolat), dan satu isolat E. coli O157:H7 resistan kolistin positif gen mcr-1. Sekuensing gen mcr-1 kemudian dianalisis di unit Biotek Balai Besar Pengujian Mutu dan Sertifikasi Obat Hewan dengan menggunakan basic local alignment search tools (BLAST) dan software MEGA7. Hasil sekuensing gen mcr-1 dengan panjang nukleotida 309 memiliki homologi tinggi dengan data referen dari Genbank pada gen mcr-1 yang terdapat dalam plasmid. Hasil sekuensing DNA gen mcr-1 sampel lebih cenderung termasuk pada tipe plasmid IncI2 atau IncHI2. Hal ini menunjukkan bahwa resistansi kolistin merupakan ancaman yang nyata karena gen resistan mcr-1 yang ada di Indonesia benar berada di plasmid sehingga mudah disebarkan ke bakteri lain. Kata kunci: mcr-1, plasmid, resistansi ABSTRACT The mobilized colistin resistance (mcr) gene is a colistin sulfate resistance gene that can be transferred through mobile genetic material such as plasmids. The purpose of this study was to determine the type of plasmid mcr-1 gene that was successfully transferred from an isolate of colistin-resistant Escherichia coli to Salmonella Enteritidis ATCC 13076 (two isolates), and one colistin-resistant E. coli O157: H7 that positive mcr-1 gene. The sequencing of the mcr-1 gene was then analyzed in the Biotek unit at National Veterinary Drug Assay Laboratory using basic local alignment search tools (BLAST) and MEGA7 software. The sequencing of the mcr-1 gene with nucleotide length 309 has a high homology with the reference data from Genbank on the mcr-1 gene contained in the plasmid. DNA sequencing of mcr-1 gene samples is more likely to belong to the IncI2 or IncHI2 plasmid types. This shows that colistine resistance is a real threat because the mcr-1 resistance gene in Indonesia is actually in the plasmid so it is easily spread to other bacteria. Keywords: mcr-1, plasmid, resistance
Variasi Respon Pembentukan IgY terhadap Toxoid Tetanus dalam Serum dan Kuning Telur pada Individu Ayam Petelur I Wayan Teguh Wibawan; Iman Bayu Prakoso Darmono; I Nyoman Suartha
Jurnal Veteriner Vol 11 No 3 (2010)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Abstract

The variation of response on the production of specific IgY to tetanus toxoid among chickenin serum and egg yolk was observed in this study. Chicken showed relatively late response inproducing specific IgY in serum, around 59 days were needed to have a positive precipitationreaction of complex IgY-tetanus toxoid in the immunodiffusion test (agar gel precipitation test/AGPT). The presence of IgY in egg yolk could be detected one week after positive reations inserum was observed. The positive reaction in AGPT mostly related with the positive reaction inELISA, eventhough the variation of titer values were observed among chicken sera and egg yolk.This response variation might be related with the different of physiological status of the chicken.
Keberhasilan Mendeteksi Gen Penyandi Resistensi Tetracycline dan Plasmid Mediated Quinolones pada Bakteri Salmonella Ayam di Bandung dan Purwakarta Leila Nur Aziah; Agustin Indrawati; I Wayan Teguh Wibawan
Jurnal Veteriner Vol 21 No 2 (2020)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Abstract

This study was aimed to identify genes encoding tetracycline and plasmid-mediated quinolones resistance to Salmonella spp from Poultry Farm in Bandung and Purwakarta, West Java. A total of 70 samples were collected from poultry farm in Bandung and Purwakarta, West Java. All isolates were test by selective media (Salmonella Shigella Agar/SSA) and confirmation Salmonella with polymerase chain reaction (PCR). Thirty three isolate positive from selective media Salmonella Shigella Agar (SSA) and 21 isolat was confirmed as Salmonella spp by PCR. A total of twenty one isolate isolated were tested for tetracycline, doxycicline,, nalidixic acid, oxytetracycline, enrofloxacyn using disk diffusion method. TEresistant were screened for presence of tet(A) and tet(B) genes by single PCR. The qnr(A), qnr(B) and qnr(S) genes were detected by multiplex PCR in quinolone resistant Salmonella isolates. The result of antibiotic sensitivity test showed that resistance to ampicillin (95.2%), tetracycline (100%), oxytetracycline (95.2%), nalidixic acid (90.4%), eritromisin (85.7%), enrofloxacin (76.2%), Gentamisin 47.6%, chloramphenicol (38.1%). The distribution of antibiotics-resistance genes in the Salmonella isolates included ampC (95.2%), tet(A)(61.9%), tet(B)(38.1%), qnr(A)(28.5%), qnr(B)(14.3%) and qnr(S)(23.8%). This study shows that a few pathogens of Salmonella are resistant to ampicillin, tetracycline , and quinolone. The tet and qnr genes are responsible for this resistance among Salmonella in Bandung and Purwakarta, West Java Indonesia was high.
Produksi IgY Antivirus Avian Influenza H5N1 dan Prospek Pemanfaatannya dalam Pengebalan Pasif I Wayan Teguh Wibawan; Sri Murtini; Retno Damajanti Soejoedono; I Gusti Ngurah Kade Mahardika
Jurnal Veteriner Vol 10 No 3 (2009)
Publisher : Faculty of Veterinary Medicine, Udayana University and Published in collaboration with the Indonesia Veterinarian Association

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Abstract

Immunoglobulin Y (IgY) in yolk has been shown in several studies to prevent both bacterial and viralinfections. This research was conducted to find evidence that IgY specific against avian influenza virus(AIV) of H5N1 subtype can be produced in a large quantity in egg yolk. Laying hens were vaccinated withAI killed-vaccine (IPB-Shigeta). The IgY was purified using affinity chromatograpy technique, and anti-H5activity was measured using a standard haemaglutination inhibition (HI) and agar gel immunodifusion.The concentration of IgY was calculated, and the protein pattern was detected using polyacrilamid gel(AGID) electrophoresis (PAGE). Anti H5 antibody as high as 27 – 29 HI units was detected and produce aspecific line of precipitation in AGID. The concentration of IgY was 7.89 mg/ml. Purified specific IgY consistof 6 main protein bands with molecular weights ranging from 35 to 225 kD. These proteins were sensitiveto heat treatment (75oC for 30 minutes), to acid condition (pH2) as well as the pepsin and trypsin. Theseresults indicated the possibility of using specific IgY for passive immunisation to prevent AIV infection oras immunotherapeutic applications for AI treatment in humans.
Co-Authors Agatha Winny Kurniatanti Sanjaya Agik Suprayogi Agnesia Endang Tri Hastuti Wahyuni Agus Setiyono Agustin Indrawati Ahmad Biharidin Ahmad Sulaeman Ahmad Sulaeman Aida Lousie Tenden Rompis Aisjah Girindra Amrozi Anak Agung Sagung Kendran Andi PM Yusmanto Andri Cahya Irawan Andrijanto Hauferson Angi ANGELA MARIANA LUSIASTUTI Anindya Kurniawati Anita Esfandiari Aprilia Hardiati Aryani Satyaningtijas Bagus Nanang Luwito Bambang Pontjo Priosoeryanto Barkah, Nisa Nurmilati BIBIANA W LAY Budi Setiawan Budi Setiawan Cece Sumantri Chaerul Basri Christoph Lammler Chusnul Choliq Citra Noviana Damiana Rita Ekastuti Darsono Darsono Debby Fadhilah Pazra Denny Widaya Lukman DEWI APRI ASTUTI Diah Iskandriati Dinar Arifianto Dinda Reisinta Dinda Reisinta Diyantoro Diyantoro Dondin Sajuthi Drajat Martiano Drajat Martianto Dwi Santy Damayati Dyah Ayu Hewajuli Dyah Ayu Hewajuli Dyah Hapsari Eka Nugraheni Ekowati Handharyani Elizabeth Wina Elsi Rahmadhani Endhie D. Setiawan Eny Palupi Erfiandini Eka Puspita Ernes Andhesfa Etih Sudarnika Evy Damayanthi Fachriyan H Pasaribu Fachriyan H. Pasaribu Fachriyan Hasmi Pasaribu Fachriyan Hasmi Pasaribu Fachriyan Hasmi Pasaribu Fachriyan Hasmi Pasaribu Fachriyan Hasmi Pasaribu Fachriyan Hasymi Pasaribu Fachriyan Pasaribu Faidah Rachmawati Rachmawati Faisal Faisal Feri Kusnandar Fitria Susanti Fitria Susanti Fitrine Ekawasti, Fitrine Gatut Ashadi Gusti Ayu Yuniati Kencana Hadi Riyadi Hadri Latif Harimurti Nuradji Harlystiarini Harlystiarini HERA MAHESHWARI Hirawan Setiadi Huda Salahuddin Darusman Huda Shalahudin Darusman I Gusti Agung Ayu Suartini I Gusti Ngurah Kade Mahardika I Gusti Ngurah Narendra Putra I Gusti Ngurah Narendra Putra I Ketut Sutama I Komang Gede Wiryawan I Made Suma Anthara I Nyoman Suarta I Nyoman Suartha I Wayan Wirata Ida Bagus Kade Suardana Iman Bayu Prakoso Darmono Indah Kusumaningrum Indrawati Sendow Isdoni Bustaman Iwan Harjono Utama Kallau, Novalino Harold Geoffrey Kamaluddin Zarkasie Kamil Riski Sidik Ketut Karuni Nyanakumari Natih Khairullah, Aswin Rafif koekoeh santoso Kris Damar Sasi Leila Nur Aziah Leila Nur Azizah LIA SITI HALIMAH Liana Verdini MAGGY T. SUHARTONO Maggy Thenawidjaja Suhartono Maharani Maharani Mahdi Abrar Mala Nurilmala Mangaraja Pidoli Tampubolon MARDHIATI, RETNO Maria Fatima Palupi Maria Fatima Palupi Maria Fatima Palupi Maria Fatima Palupi Michael Haryadi Wibowo Mira Mawardi Mirnawati Baharudin Sudarwanto Mirnawati Baharudin Sudarwanto Mirnawati Soedarwanto Mirnawati Soedarwanto Mirnawati Sudarwanto Mohammad Ashraf Muhammad Rivai Muharam Saepulloh Muhsinin, Muhammad Nahrowi Nahrowi Ni Luh Putu Agustini Ni Luh Putu Ika Mayasari Ni Luh Putu Indi Dharmayanti Ni Made Ritha Krisna Dewi Ni Made Ritha Krisna Dewi Niken Ulupi NLP Indi Dharmayanti Nurbani Kalsum Okti Nadia Poetri Pamungkas, Joko Puarada, Alif Rahman Rohim Pudji Achmadi Purba, Hastuti Handayani S. R Susanti Ratu Shinta Mayasari Retno Damajanti Soejoedono Retno Damajanti Soejoedono Retno Damajanti Soejoedono Retno Damayanti Soejoedono Retno Mardhiati Retno Setyaningsih Retno Setyaningsih Retno Wulansari Rifky Rizkiantino Rifky Rizkiantino Rifky Rizkiantino Risma Juniarti Paulina Silitonga Rita Mutia Rizal Rahadian Ramdhany Ronald Tarigan Ruben Hasiholan Panggabean Rudi Rawendra Safika S, Safika Seruni Agistiana Setyo Widodo Setyo Widodo Siti Gusti Ningrum Siti Gusti Ningrum Siti Madanijah Siti Madanijah Sri Anna Marliyati Sri Budiarti Poerwanto sri murtini . Sri Suryatmiati Prihandani Sriyanto Sriyanto Sriyanto Sriyanto Sucitya Purnama Supar - Surachmi Setiyaningsih Sus Derthi Widhyari Susan Maphilindawati Noor Sylvia Oscarina Teuku Fadrial Karmil Titiek Djannatun Tiurma Sinaga Trioso Purnawarman Veybe G. Kereh Wendy Setiyadi Putranto Widya Hermana Wyanda Arnafia Wyanda Arnafia Wyanda Arnafia Wyanda Arnafia Yuli Retnani Yunetta Putri Arios Yusnani - Zinatul Hayati